Stra13 regulates oxidative stress mediated skeletal muscle degeneration

被引:34
作者
Vercherat, Cecile [1 ]
Chung, Teng-Kai [1 ,3 ]
Yalcin, Safak [2 ]
Gulbagci, Neriman [1 ]
Gopinadhan, Suma [3 ]
Ghaffari, Saghi [1 ,2 ]
Taneja, Reshma [1 ,3 ,4 ]
机构
[1] Mt Sinai Sch Med, Dept Dev & Regenerat Biol, New York, NY USA
[2] Mt Sinai Sch Med, Dept Gene & Cell Med, New York, NY USA
[3] Natl Univ Singapore, Dept Physiol, Singapore 117597, Singapore
[4] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore 117597, Singapore
关键词
DUCHENNE MUSCULAR-DYSTROPHY; INDUCED APOPTOSIS; HEME OXYGENASE-1; MDX MOUSE; TNF-ALPHA; GLYCOPROTEIN COMPLEX; CELL ACTIVATION; MICE; EXPRESSION; GENE;
D O I
10.1093/hmg/ddp383
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Duchenne Muscular Dystrophy (DMD), caused by loss of dystrophin is characterized by progressive muscle cell necrosis. However, the mechanisms leading to muscle degeneration in DMD are poorly understood. Here, we demonstrate that Stra13 protects muscle cells from oxidative damage, and its absence leads to muscle necrosis in response to injury in Stra13-deficient mice. Interestingly, Stra13-/- mutants express elevated levels of TNF alpha, reduced levels of heme-oxygenase-1, and display apparent signs of oxidative stress prior to muscle death. Moreover, Stra13-/- muscle cells exhibit an increased sensitivity to pro-oxidants, and conversely, Stra13 overexpression provides resistance to oxidative damage. Consistently, treatment with antioxidant N-acetylcysteine ameliorates muscle necrosis in Stra13-/- mice. We also demonstrate that Stra13 expression is elevated in muscles from dystrophin-deficient (mdx) mice, and mdx/Stra13-/- double mutants exhibit an early onset of muscle degeneration. Our studies underscore the importance of oxidative stress-mediated muscle degeneration in muscular dystrophy, and reveal the contribution of Stra13 in maintenance of muscle integrity.
引用
收藏
页码:4304 / 4316
页数:13
相关论文
共 48 条
[1]   Stra13, a prostaglandin E2-induced gene, regulates the cellular redox state of podocytes [J].
Bek, MJ ;
Wahle, S ;
Müller, B ;
Benzing, T ;
Huber, TB ;
Kretzler, M ;
Cohen, C ;
Busse-Grawitz, A ;
Pavenstadt, H .
FASEB JOURNAL, 2003, 17 (02) :682-+
[2]   TOCOPHEROL DEFICIENCY IN MAN [J].
BINDER, HJ ;
HERTING, DC ;
HURST, V ;
FINCH, SC ;
SPIRO, HM .
NEW ENGLAND JOURNAL OF MEDICINE, 1965, 273 (24) :1289-&
[3]   Function and genetics of dystrophin and dystrophin-related proteins in muscle [J].
Blake, DJ ;
Weir, A ;
Newey, SE ;
Davies, KE .
PHYSIOLOGICAL REVIEWS, 2002, 82 (02) :291-329
[4]   INTRACELLULAR CALCIUM ACCUMULATION IN DUCHENNE DYSTROPHY AND OTHER MYOPATHIES - STUDY OF 567,000 MUSCLE-FIBERS IN 114 BIOPSIES [J].
BODENSTEINER, JB ;
ENGEL, AG .
NEUROLOGY, 1978, 28 (05) :439-446
[5]   Overexpression of Stra13 a novel retinoic acid-inducible gene of the basic helix-loop-helix family, inhibits mesodermal and promotes neuronal differentiation of P19 cells [J].
Boudjelal, M ;
Taneja, R ;
Matsubara, S ;
Bouillet, P ;
Dolle, P ;
Chambon, P .
GENES & DEVELOPMENT, 1997, 11 (16) :2052-2065
[6]   X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].
BULFIELD, G ;
SILLER, WG ;
WIGHT, PAL ;
MOORE, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192
[7]   Peroxiredoxin III, a mitochondrion-specific peroxidase, regulates apoptotic signaling by mitochondria [J].
Chang, TS ;
Cho, CS ;
Park, S ;
Yu, SQ ;
Kang, SW ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) :41975-41984
[8]   Tumor necrosis factor-α gene transfer induces cachexia and inhibits muscle regeneration [J].
Coletti, D ;
Moresi, V ;
Adamo, S ;
Molinaro, M ;
Sassoon, D .
GENESIS, 2005, 43 (03) :120-128
[9]   Molecular mechanisms of muscular dystrophies: old and new players [J].
Davies, Kay E. ;
Nowak, Kristen J. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (10) :762-773
[10]   Evidence of oxidative stress in mdx mouse muscle:: Studies of the pre-necrotic state [J].
Disatnik, MH ;
Dhawan, J ;
Yu, Y ;
Beal, MF ;
Whirl, MM ;
Franco, AA ;
Rando, TA .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 161 (01) :77-84